UIH recalls Positron Emission Tomography and Computed Tomography System model uEXPLORER MD for potential mechanical interference during patient table movement.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH is recalling its Positron Emission Tomography and Computed Tomography System model uEXPLOR: third-party outer covers can trap between patient table and gantry, causing mechanical interference during table movement. This could lead to safety issues during medical procedures.
Third-party outer covers can become trapped between the patient table and gantry during movement. This mechanical interference may cause safety issues during medical imaging procedures.
Medical facilities using the uEXPLORER MD model with serial numbers F00002 or F00015 are affected. Patients and staff at these facilities are at risk during imaging procedures.
Check for the model uEXPLORER MD with serial numbers F00002 or F00015. The product was sold by Shanghai United Imaging Healthcare Co., Ltd. in the U.S.
Identify if your system has serial numbers F00002 or F00015 and model uEXPLORER MD.
The recall indicates a potential hazard, but the product is not unsafe unless the specific issue occurs. Follow the action steps to ensure safety.
Check if your system has serial numbers F00002 or F00015 and model uEXPLORER MD. If affected, contact UIH Technologies for further instructions.
The recall record does not specify a remedy, so no immediate fix is provided. Contact UIH Technologies for guidance.
We’ve drafted a message you can send UIH Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0222-2026 — UIH Technologies UIH Technologies Hello, I own a UIH Technologies that is covered by recall Z-0222-2026 from UIH Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
